Disability and lesion load in MS: a reassessment with MS functional composite score and 3D fast FLAIR

被引:37
作者
Ciccarelli, O [1 ]
Brex, PA [1 ]
Thompson, AJ [1 ]
Miller, DH [1 ]
机构
[1] UCL Inst Neurol, NMR Res Unit, London WC1N 3BG, England
关键词
multiple sclerosis; magnetic resonance imaging; clinical evaluation;
D O I
10.1007/PL00007843
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The correlation between T2 lesion load (LL) detected on conventional MR sequences and disability assessed by the Expanded Disability Status Scale (EDSS) in multiple sclerosis (MS) is, at best, moderate. The present study was performed to determine whether the correlation between disability and LL is improved by (i) use of the more sensitive three-dimensional fast fluid-attenuated inversion recovery (3D-fast FLAIR) sequence; (ii) application of the newly devised MS functional composite (MSFC) score. Forty-one patients with clinically definite or probable MS were studied. All had been followed prospectively for 14 years since their first symptom. EDSS and MSFC score were,assessed. Imaging was performed with 3D-fFLAIR, fast spin-echo (FSE), and T1 weighted SE sequences. 3D-fFLAIR detected a 34% higher LL than FSE, but did not improve the correlation between T2 LL and EDSS (r=0.51 and r=0.53); the correlation was stronger with T1 LL (r=0.57). The MSFC score did not significantly correlate with T2 LL or T1 LL. The robust correlation in this cohort between T2 LL and EDSS may reflect the homogeneous disease duration and the wide spread of disability. This correlation was not improved by the increased detection of T2 lesions with the 3D-fFLAIR sequence. The stronger correlation between T1 LL with EDSS is consistent with the finding that this subgroup of lesions represent areas of more severe tissue damage. The MSFC score did not improve the clinico-radiological paradox that is found in MS, despite including information on cognitive function.
引用
收藏
页码:18 / 24
页数:7
相关论文
共 40 条
[1]  
[Anonymous], 1999, Administration and scoring manual for the multiple sclerosis functional composite measure (MSFC)
[2]   3D fast FLAIR: A CSF-nulled 3D fast spin-echo pulse sequence [J].
Barker, GJB .
MAGNETIC RESONANCE IMAGING, 1998, 16 (07) :715-720
[3]   MRI in multiple sclerosis: correlation with expanded disability status scale (EDSS) [J].
Barkhof, F .
MULTIPLE SCLEROSIS JOURNAL, 1999, 5 (04) :283-286
[4]  
Bastianello S, 1997, AM J NEURORADIOL, V18, P699
[5]   Comfortable and maximum walking speed of adults aged 20-79 years: Reference values and determinants [J].
Bohannon, RW .
AGE AND AGEING, 1997, 26 (01) :15-19
[6]   Lesion heterogeneity in multiple sclerosis: a study of the relations between appearances on T1 weighted images, T1 relaxation times, and metabolite concentrations [J].
Brex, PA ;
Parker, GJM ;
Leary, SM ;
Molyneux, PD ;
Barker, GJ ;
Davie, CA ;
Thompson, AJ ;
Miller, DH .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2000, 68 (05) :627-632
[7]   Intrarater and interrater reliability of the MS functional composite outcome measure [J].
Cohen, JA ;
Fischer, JS ;
Bolibrush, DM ;
Jak, AJ ;
Kniker, JE ;
Mertz, LA ;
Skaramagas, TT ;
Cutter, GR .
NEUROLOGY, 2000, 54 (04) :802-806
[8]   Development of a multiple sclerosis functional composite as a clinical trial outcome measure [J].
Cutter, GR ;
Baier, ML ;
Rudick, RA ;
Cookfair, DL ;
Fischer, JS ;
Petkau, J ;
Syndulko, K ;
Weinshenker, BG ;
Antel, JP ;
Confavreux, C ;
Ellison, GW ;
Lublin, F ;
Miller, AE ;
Rao, SM ;
Reingold, S ;
Thompson, A ;
Willoughby, E .
BRAIN, 1999, 122 :871-882
[9]   CLINICALLY ISOLATED LESIONS OF THE TYPE SEEN IN MULTIPLE-SCLEROSIS - A COGNITIVE, PSYCHIATRIC, AND MRI FOLLOW-UP-STUDY [J].
FEINSTEIN, A ;
KARTSOUNIS, LD ;
MILLER, DH ;
YOUL, BD ;
RON, MA .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1992, 55 (10) :869-876
[10]   Quantitative assessment of MRI lesion load in multiple sclerosis - A comparison of conventional spin-echo with fast fluid-attenuated inversion recovery [J].
Filippi, M ;
Yousry, T ;
Baratti, C ;
Horsfield, MA ;
Mammi, S ;
Becker, C ;
Voltz, R ;
Spuler, S ;
Campi, A ;
Reiser, MF ;
Comi, G .
BRAIN, 1996, 119 :1349-1355